Abstract

BackgroundUnbalanced dietary intakes of saturated (SFAs) and polyunsaturated (PUFAs) fatty acids can profoundly influence the hypothalamic-pituitary-adrenal (HPA)-axis and glucocorticoid secretions in relation to behavioral performances. The beneficial effects of higher dietary PUFA intakes and PUFA:SFA ratios may also affect social interactions and social-living per se, where adequate physiological and behavioral responses are essential to cope with unstable social environmental conditions.MethodsEffects of diets high in PUFAs or SFAs and a control diet were investigated in male and female guinea pigs after 60 days of supplementation. Plasma fatty acid patterns served as an indicator of the general fatty acid status. HPA-axis activities, determined by measuring saliva cortisol concentrations, social behaviors, and hierarchy ranks were analyzed during group housing of established single-sexed groups and during challenging social confrontations with unfamiliar individuals of the other groups.ResultsThe plasma PUFA:SFA ratio was highest in PUFA supplemented animals, with female levels significantly exceeding males, and lowest in SFA animals. SFA males and females showed increased saliva cortisol levels and decreased aggressiveness during group housing, while sociopositive behaviors were lowest in PUFA males. Males generally showed higher cortisol increases in response to the challenging social confrontations with unfamiliar individuals than females. While increasing cortisol concentrations were detected in control and PUFA animals, no such effect was found in SFA animals. During social confrontations, PUFA males showed higher levels of agonistic and sociopositive behaviors and also gained higher dominance ranks among males, which was not detected for females.ConclusionsWhile SFAs seemingly impaired cortisol responses and social behaviors, PUFAs enabled adequate behavioral responses in male individuals under stressful new social environmental conditions. This sex-specific effect was possibly related to a general sex difference in the n-3 PUFA bioavailability and cortisol responses, which may indicate that males are more susceptible to changing environmental conditions, and shows how dietary fatty acids can shape social systems.Electronic supplementary materialThe online version of this article (doi:10.1186/s13293-016-0107-5) contains supplementary material, which is available to authorized users.

Highlights

  • Unbalanced dietary intakes of saturated (SFAs) and polyunsaturated (PUFAs) fatty acids can profoundly influence the hypothalamic-pituitary-adrenal (HPA)-axis and glucocorticoid secretions in relation to behavioral performances

  • The present study aimed to extend the findings on the modulatory influences of dietary fatty acids by comparing the effects of Polyunsaturated fatty acid (PUFA) and Saturated fatty acid (SFA) on saliva cortisol concentrations and social behaviors in male and female domestic guinea pigs (Cavia aperea f. porcellus) under different social conditions

  • Total plasma n-3 and n-6 fatty acids were highest in animals fed on the high-PUFA diet, with PUFA males showing lower n-3 levels than PUFA

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Summary

Introduction

Unbalanced dietary intakes of saturated (SFAs) and polyunsaturated (PUFAs) fatty acids can profoundly influence the hypothalamic-pituitary-adrenal (HPA)-axis and glucocorticoid secretions in relation to behavioral performances. Considering the general benefits of lower dietary n-6:n-3 ratios for neurophysiological processes [10, 11], PUFAs can positively affect a variety of brain-related behavioral functions [12, 13], while the opposite may be the case for elevated dietary intakes of non-essential SFAs [14] In this context, it has been shown that dietary supplementations with the n-3 PUFAs ALA or DHA can both diminish glucocorticoid secretion rates and related stress-induced anxiety- and depressive-like behaviors and cognitive impairments in rats [15, 16]. These physiological and behavioral impacts are probably linked to the adverse effects of dietary PUFAs and SFAs on the availability, accumulation, and incorporation of long-chain PUFAs in the hippocampus and hypothalamus and neurotransmitter signaling in these brain areas [20, 21]

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